Canonical Allele Identifier: CA891837958

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965414_87965415delinsAA , CM000672.2:g.87965414_87965415delinsAA	GRCh38
NC_000010.10:g.89725171_89725172delinsAA , CM000672.1:g.89725171_89725172delinsAA	GRCh37
NC_000010.9:g.89715151_89715152delinsAA	NCBI36
NG_007466.2:g.106976_106977delinsAA , LRG_311:g.106976_106977delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1247_1248delinsAA	ENSP00000514759.2:p.Ser416Ter
ENST00000710265.1:c.*183_*184delinsAA	ENSP00000518161.1:n.*183_*184delinsAA
ENST00000688158.2:n.1889_1890delinsAA
ENST00000688922.2:c.*984_*985delinsAA	ENSP00000508742.2:n.*984_*985delinsAA
ENST00000700021.1:c.1109_1110delinsAA	ENSP00000514757.1:p.Ser370Ter
ENST00000700022.1:c.*493_*494delinsAA	ENSP00000514758.1:n.*493_*494delinsAA
ENST00000700023.1:n.2312_2313delinsAA
ENST00000700024.1:n.2546_2547delinsAA
ENST00000706954.1:c.1154_1155delinsAA	ENSP00000516674.1:p.Ser385Ter
ENST00000706955.1:c.*1189_*1190delinsAA	ENSP00000516675.1:n.*1189_*1190delinsAA
ENST00000686459.1:c.*740_*741delinsAA	ENSP00000508909.1:n.*740_*741delinsAA
ENST00000688158.1:c.*1265_*1266delinsAA	ENSP00000509254.1:n.*1265_*1266delinsAA
ENST00000688308.1:c.1154_1155delinsAA	ENSP00000508752.1:p.Ser385Ter
ENST00000688922.1:c.1075_1076delinsAA
ENST00000693560.1:c.1673_1674delinsAA	ENSP00000509861.1:p.Ser558Ter
ENST00000371953.8:c.1154_1155delinsAA MANE Select	ENSP00000361021.3:p.Ser385Ter
ENST00000371953.7:c.1154_1155delinsAA	ENSP00000361021.3:p.Ser385Ter
NM_000314.5:c.1154_1155delinsAA	NP_000305.3:p.Ser385Ter
NM_000314.6:c.1154_1155delinsAA	NP_000305.3:p.Ser385Ter
NM_001304717.2:c.1673_1674delinsAA	NP_001291646.2:p.Ser558Ter
NM_001304718.1:c.563_564delinsAA	NP_001291647.1:p.Ser188Ter
XM_006717926.2:c.1109_1110delinsAA	XP_006717989.1:p.Ser370Ter
XM_011539982.1:c.1058_1059delinsAA	XP_011538284.1:p.Ser353Ter
XR_945791.1:n.1724_1725delinsAA
NM_000314.7:c.1154_1155delinsAA	NP_000305.3:p.Ser385Ter
NM_001304717.5:c.1673_1674delinsAA	NP_001291646.4:p.Ser558Ter
NM_001304718.2:c.563_564delinsAA	NP_001291647.1:p.Ser188Ter
NM_000314.8:c.1154_1155delinsAA MANE Select	NP_000305.3:p.Ser385Ter